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DNA Repair Protein Complementing XP-G Cells (ERCC5) Antibody

DNA Repair Protein Complementing XP-G Cells (ERCC5) Antibody

Manufacturer	Abbexa
Category	Oncology Antibodies By Cell Type Carcinoma Hematology Lymphoma Sarcoma Western Blot Primary Antibodies
Type	Antibody Primary
Specific against	Human
Isotype	IgG
Applications	WB
Amount	400 ul
Host	Rabbit
Item no.	abx029850-400
Targets	ERCC5
Conjugate/Tag	Unconjugated
eClass 6.1	32160702
eClass 9.0	32160702
Available
Antigen	ERCC5
Description	Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined. [provided by RefSeq].
Conjugation	Unconjugated
Purification	Purified through a protein A column, followed by peptide affinity purification.
Storage	Aliquot and store at -20C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC	P28715
UniProt Entry Name	ERCC5_HUMAN
Gene Symbol	ERCC5
Buffer	PBS containing 0.09% sodium azide.
Dry Ice	No
Note	This product is for research use only.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

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